ClinVar Miner

Submissions for variant NM_005458.8(GABBR2):c.460-20G>A

dbSNP: rs2490087298
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003031506 SCV003320758 likely benign Epileptic encephalopathy 2022-03-23 criteria provided, single submitter clinical testing

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